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高原适应过程中的血栓弹力描记术和血小板功能。

Thromboelastometry and Platelet Function during Acclimatization to High Altitude.

机构信息

Apex (Altitude Physiology Expeditions), Edinburgh, United Kingdom.

Edinburgh Medical School, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

Thromb Haemost. 2018 Jan;118(1):63-71. doi: 10.1160/TH17-02-0138. Epub 2018 Jan 5.

Abstract

Interaction between hypoxia and coagulation is important given the increased risk of thrombotic diseases in chronically hypoxic patients who reside at sea level and in residents at high altitude. Hypoxia alters the proteome of platelets favouring a prothrombotic phenotype, but studies of activation and consumption of specific coagulation factors in hypoxic humans have yielded conflicting results. We tested blood from 63 healthy lowland volunteers acclimatizing to high altitude (5,200 m) using thromboelastometry and assays of platelet function to examine the effects of hypoxia on haemostasis. Using data from two separate cohorts of patients following identical ascent profiles, we detected a significant delay in clot formation, but increased clot strength by day 7 at 5,200 m. The latter finding may be accounted for by the significant rise in platelet count and fibrinogen concentration that occurred during acclimatization. Platelet function assays revealed evidence of platelet hyper-reactivity, with shortened PFA-100 closure times and increased platelet aggregation in response to adenosine diphosphate. Post-expedition results were consistent with the normalization of coagulation following descent to sea level. These robust findings indicate that hypoxia increases platelet reactivity and, with the exception of the paradoxical delay in thromboelastometry clotting time, suggest a prothrombotic phenotype at altitude. Further work to elucidate the mechanism of platelet activation in hypoxia will be important and could impact upon the management of patients with acute or chronic hypoxic respiratory diseases who are at risk of thrombotic events.

摘要

鉴于居住在海平面和高海拔地区的慢性低氧患者发生血栓性疾病的风险增加,缺氧与凝血之间的相互作用非常重要。缺氧改变了血小板的蛋白质组,有利于形成促血栓形成表型,但对低氧状态下人类特定凝血因子的激活和消耗的研究结果却存在矛盾。我们使用血栓弹力描记术和血小板功能检测,对 63 名来自低海拔地区的健康志愿者(在海拔 5200 米处适应高海拔环境)的血液进行了检测,以研究缺氧对止血的影响。通过对两个采用相同上升模式的患者队列的数据进行分析,我们发现,在海拔 5200 米时,凝血形成的时间明显延迟,但血块强度在第 7 天增加。后者的发现可能与在适应过程中血小板计数和纤维蛋白原浓度的显著增加有关。血小板功能检测显示出血小板过度反应的证据,血小板聚集物反应性增加,血小板聚集物对二磷酸腺苷的反应性增加,PFA-100 关闭时间缩短。远征后的结果与返回海平面后凝血正常化的结果一致。这些可靠的发现表明,缺氧会增加血小板的反应性,除了血栓弹力描记法凝血时间的反常延迟外,这表明在高海拔环境下存在促血栓形成表型。进一步阐明缺氧状态下血小板激活的机制非常重要,这可能会影响到有发生血栓性事件风险的急性或慢性低氧性呼吸系统疾病患者的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f0/6260116/cfe636564151/10-1160-th17-02-0138-i170138-1.jpg

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